RESUMEN
The stratum corneum is the outermost skin layer with a vital role in skin barrier function. It is comprised of dead keratinocytes (corneocytes) and is known to maintain its thickness by shedding cells, although, the precise mechanisms that safeguard stratum corneum maturation and homeostasis remain unclear. Previous ex vivo studies have suggested a neutral-to-acidic pH gradient in the stratum corneum. Here, we use intravital pH imaging at single-corneocyte resolution to demonstrate that corneocytes actually undergo differentiation to develop three distinct zones in the stratum corneum, each with a distinct pH value. We identified a moderately acidic lower, an acidic middle, and a pH-neutral upper layer in the stratum corneum, with tight junctions playing a key role in their development. The upper pH neutral zone can adjust its pH according to the external environment and has a neutral pH under steady-state conditions owing to the influence of skin microbiota. The middle acidic pH zone provides a defensive barrier against pathogens. With mathematical modeling, we demonstrate the controlled protease activation of kallikrein-related peptidases on the stratum corneum surface that results in proper corneocyte shedding in desquamation. This work adds crucial information to our understanding of how stratum corneum homeostasis is maintained.
Asunto(s)
Epidermis , Homeostasis , Queratinocitos , Concentración de Iones de Hidrógeno , Animales , Queratinocitos/metabolismo , Epidermis/metabolismo , Piel/metabolismo , Ratones , Humanos , Diferenciación Celular , Uniones Estrechas/metabolismo , Masculino , Femenino , Ratones Endogámicos C57BLRESUMEN
Extramammary Paget disease (EMPD) is an intraepithelial adenocarcinoma that primarily affects the genital and axillary areas in older individuals. A limited number of paired patients with familial EMPD (i.e. parent-offspring, siblings) have been reported but the genetics have not yet been adequately studied. We report, to the best of our knowledge, the first familial cases of patients with EMPD involving three affected siblings. The tumour-only multigene panel testing using surgical specimens revealed a heterozygous c.2997A>C (p.Glu999Asp) nonsynonymous variant in the proto-oncogene MET (NM_000245.4) in the three affected siblings. The germline multigene panel testing using peripheral blood lymphocytes revealed the same missense MET variant in all five family members who were tested, including two asymptomatic offspring (51 and 37â years of age). The MET variant we identified could be involved in EMPD carcinogenesis. Further genomic analyses of patients with familial EMPD are warranted to validate the pathogenic relevance of MET variants in EMPD development.
Asunto(s)
Enfermedad de Paget Extramamaria , Proto-Oncogenes Mas , Proteínas Proto-Oncogénicas c-met , Hermanos , Humanos , Masculino , Enfermedad de Paget Extramamaria/genética , Enfermedad de Paget Extramamaria/patología , Persona de Mediana Edad , Femenino , Proteínas Proto-Oncogénicas c-met/genética , Adulto , Mutación Missense , Neoplasias Cutáneas/genética , Neoplasias Cutáneas/patología , Anciano , LinajeAsunto(s)
Ictiosis Lamelar , Ictiosis , Epidermis , Humanos , Ictiosis/genética , Inflamación/genéticaRESUMEN
Tinea imbricata and tinea pseudoimbricata are variant types of tinea corporis characterized by annual-ring-shaped erythema. Although the skin lesions manifest similar symptoms, these two diseases are classified based on causative fungi. The former is caused by Trichophyton concentricum, an anthropophilic dermatophyte, and the latter is caused by dermatophytes other than T. concentricum, commonly zoophilic fungi such as Trichophyton mentagrophytes complex. Here, we report a 27-year-old Japanese male diagnosed with tinea pseudoimbricata attributed to Trichophyton tonsurans, an anthropophilic dermatophyte. We suspected that application of steroid ointment caused the annular pattern of his skin lesions. After three months use of topical luliconazole cream, treatment was finished. We also summarize the knowledge about tinea pseudoimbricata through previous reports with bibliographical consideration.
Asunto(s)
Arthrodermataceae , Tiña , Adulto , Humanos , Masculino , Esteroides , Tiña/diagnóstico , Tiña/tratamiento farmacológico , TrichophytonRESUMEN
Host-microbe interactions orchestrate skin homeostasis, the dysregulation of which has been implicated in chronic inflammatory conditions such as atopic dermatitis and psoriasis. Here, we show that Staphylococcus cohnii is a skin commensal capable of beneficially inhibiting skin inflammation. We find that Tmem79-/- mice spontaneously develop interleukin-17 (IL-17)-producing T-cell-driven skin inflammation. Comparative skin microbiome analysis reveals that the disease activity index is negatively associated with S. cohnii. Inoculation with S. cohnii strains isolated from either mouse or human skin microbiota significantly prevents and ameliorates dermatitis in Tmem79-/- mice without affecting pathobiont burden. S. cohnii colonization is accompanied by activation of host glucocorticoid-related pathways and induction of anti-inflammatory genes in the skin and is therefore effective at suppressing inflammation in diverse pathobiont-independent dermatitis models, including chemically induced, type 17, and type 2 immune-driven models. As such, S. cohnii strains have great potential as effective live biotherapeutics for skin inflammation.
Asunto(s)
Inflamación/inmunología , Piel/patología , Staphylococcus/metabolismo , Animales , Humanos , RatonesAsunto(s)
Alopecia Areata/patología , Poliposis Intestinal/patología , Pólipos Intestinales/patología , Prednisolona/uso terapéutico , Administración Oral , Alopecia Areata/diagnóstico , Alopecia Areata/fisiopatología , Biopsia con Aguja , Dermoscopía/métodos , Endoscopía Gastrointestinal/métodos , Humanos , Inmunohistoquímica , Poliposis Intestinal/diagnóstico , Pólipos Intestinales/diagnóstico , Masculino , Persona de Mediana Edad , Pronóstico , Enfermedades Raras , Resultado del TratamientoRESUMEN
Both medallion-like dermal dendrocyte hamartoma and fibroblastic connective tissue nevus are rare benign dermal lesions composed of CD34-positive spindle cells. Although regarded as different diseases, it is sometimes difficult to distinguish between them due to their clinical and pathological similarities. We present a case of medallion-like dermal dendrocyte hamartoma that could also be diagnosed as fibroblastic connective tissue nevus and propose the possibility of overlap in these diseases.